US8691812B2 - Pesticidal composition and its use - Google Patents
Pesticidal composition and its use Download PDFInfo
- Publication number
- US8691812B2 US8691812B2 US13/643,576 US201113643576A US8691812B2 US 8691812 B2 US8691812 B2 US 8691812B2 US 201113643576 A US201113643576 A US 201113643576A US 8691812 B2 US8691812 B2 US 8691812B2
- Authority
- US
- United States
- Prior art keywords
- carboxamide compound
- parts
- composition
- compound
- plant
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 0 [1*]C1=C(C(=O)NC2=CC=CC3=C2C(C)CC3(C)C)C([2*])=NN1C Chemical compound [1*]C1=C(C(=O)NC2=CC=CC3=C2C(C)CC3(C)C)C([2*])=NN1C 0.000 description 4
- YJLAYFZJVNMMQB-UHFFFAOYSA-N CC1CC(C)(C)C2=C1C(NC(=O)C1=CN(C)N=C1[H]C(F)F)=CC=C2 Chemical compound CC1CC(C)(C)C2=C1C(NC(=O)C1=CN(C)N=C1[H]C(F)F)=CC=C2 YJLAYFZJVNMMQB-UHFFFAOYSA-N 0.000 description 3
- MEUXXHGDZUDAAW-UHFFFAOYSA-N CC1=NN(C)C(C)=C1C(=O)NC1=CC=CC2=C1C(C)CC2(C)C Chemical compound CC1=NN(C)C(C)=C1C(=O)NC1=CC=CC2=C1C(C)CC2(C)C MEUXXHGDZUDAAW-UHFFFAOYSA-N 0.000 description 2
- QYPFLRIVEVOAGA-UHFFFAOYSA-N CC1=NN(C)C=C1C(=O)NC1=CC=CC2=C1C(C)CC2(C)C Chemical compound CC1=NN(C)C=C1C(=O)NC1=CC=CC2=C1C(C)CC2(C)C QYPFLRIVEVOAGA-UHFFFAOYSA-N 0.000 description 2
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/12—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings condensed with a carbocyclic ring
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/22—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom rings with more than six members
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N51/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic ring
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N2300/00—Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48
Definitions
- the present invention relates to a pesticidal composition and its use.
- An object of the present invention is to provide a composition having an excellent pesticidal effect.
- the inventor of the present invention studied for seeking a composition having an excellent pesticidal effect and found that a composition comprising a carboxamide compound represented by following formula (I) and one or more neonicotinoid compounds selected from the following group (A) has an excellent pesticidal effect and then completed the present invention.
- a composition comprising a carboxamide compound represented by following formula (I) and one or more neonicotinoid compounds selected from the following group (A) has an excellent pesticidal effect and then completed the present invention.
- the present invention provides the following [1] to [7].
- a pesticidal composition comprising a carboxamide compound represented by formula (I):
- R 1 represents a hydrogen atom or a methyl group
- R 2 represents a methyl group, a difluoromethyl group or a trifluoromethyl group, and one or more neonicotinoid compounds selected from group (A) consisting of acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, thiacloprid and thiamethoxam.
- a method of controlling pest which comprises a step of treating a plant or the soil where a plant grows with an effective amount of a carboxamide compound represented by formula (I):
- R 1 represents a hydrogen atom or a methyl group
- R 2 represents a methyl group, a difluoromethyl group or a trifluoromethyl group, and one or more neonicotinoid compounds selected from group (A) consisting of acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, thiacloprid and thiamethoxam.
- various pests can be controlled.
- composition comprises a carboxamide compound represented by formula (I):
- R 1 and R 2 represent the same meanings as defined in the above (hereinafter referred to as “carboxamide compound”)
- neonicotinoid compound selected from group (A) consisting of acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, thiacloprid and thiamethoxam (hereinafter referred to as “neonicotinoid compound”).
- the “carboxamide compounds” are those as described in, for example, WO86/02641 or WO92/12970, and can be prepared by the method described therein.
- carboxamide compound (2) (hereinafter referred to as “carboxamide compound (2)”); carboxamide compound represented by formula (3):
- the “neonicotinoid compounds” are known compounds and described in, for example, “THE PESTICIDE MANUAL—14th EDITION (published by BCPC) ISBN 1901396142. These compounds can be obtained from the products containing said “neonicotinoid compound” in the market or can be synthesized by publicly known methods.
- the weight ratio of the “carboxamide compound” to the “neonicotinoid compound(s)” in the “composition” is usually from 0.01/1 to 500/1 and preferably from 0.01/1 to 4/1 of “carboxamide compound”/“neonicotinoid compound(s)”
- composition may be a mixture itself of a “carboxamide compound” and “neonicotinoid compound(s)”
- the “composition” is usually prepared by mixing a “carboxamide compound”, “neonicotinoid compound(s)” and an inert carrier, and if necessary, by adding a surfactant and/or another auxiliary for formulation and by formulating the mixture into oil formulation, emulsifiable concentrate, flowable formulation, wettable powder, water dispersible granules, powder, granules, or the like.
- the formulation which is used alone or by adding another inert component, can be used as a pesticide.
- the total content of a “carboxamide compound” and “neonicotinoid compound(s)” in a “composition” is usually from 0.1 to 99% by weight, preferably from 0.2 to 90% by weight, and more preferably from 1 to 80% by weight.
- solid carriers used for the formulation include fine powder or granules of, for example, mineral materials such as kaolin clay, attapulgite, bentonite, montmorillonite, acid clay, pyrophillite, talc, diatomaceous earth, and calcite; natural organic materials such as corncob powder, and walnut powder; synthesized organic materials such as urea; salts such as potassium carbonate, and ammonium sulfate; synthetic inorganic materials such as synthesized hydrous silicon oxide.
- mineral materials such as kaolin clay, attapulgite, bentonite, montmorillonite, acid clay, pyrophillite, talc, diatomaceous earth, and calcite
- natural organic materials such as corncob powder, and walnut powder
- synthesized organic materials such as urea
- salts such as potassium carbonate, and ammonium sulfate
- synthetic inorganic materials such as synthesized hydrous silicon oxide.
- liquid carriers examples include aromatic hydrocarbons such as xylene, alkylbenzene, and methylnaphthalene; alcohols such as 2-propanol, ethylene glycol, propylene glycol, and ethylene glycol mono-ethyl ether; ketones such as acetone, cyclohexanone, and isophorone; vegetable oils such as soybean oil, cotton seed oil; petrolic aliphatic hydrocarbons; esters; dimethylsulfoxide; acetonitrile; water.
- aromatic hydrocarbons such as xylene, alkylbenzene, and methylnaphthalene
- alcohols such as 2-propanol, ethylene glycol, propylene glycol, and ethylene glycol mono-ethyl ether
- ketones such as acetone, cyclohexanone, and isophorone
- vegetable oils such as soybean oil, cotton seed oil
- petrolic aliphatic hydrocarbons esters
- dimethylsulfoxide acetonitrile
- surfactants examples include anionic surfactants such as alkyl sulfate ester salts, alkylarylsulfonate salts, dialkylsulfosuccinate salts, polyoxyethylene alkylaryl ether phosphoric acid ester salts, lignin sulfonate, and naphthalene sulfonate formaldehyde polycondensed products; non-ionic surfactants such as polyoxyethylene alkyl aryl ethers, polyoxyethylene alkyl polyoxypropylene block copolymers, and sorbitan fatty acid esters; and cationic surfactants such as alkyl trimethyl ammonium salts.
- anionic surfactants such as alkyl sulfate ester salts, alkylarylsulfonate salts, dialkylsulfosuccinate salts, polyoxyethylene alkylaryl ether phosphoric acid ester salts, lignin sulfonate, and naphthal
- auxiliaries for formulation examples include water-soluble polymers such as polyvinyl alcohol, and polyvinylpyrrolidone; polysaccharides such as gum arabic, alginic acid and its salt, CMC (carboxymethylcellulose), and xanthan gum; inorganic materials such as aluminum magnesium silicate, alumina sol; preservatives; coloring agents;, and stabilizers such as PAP (acidic isopropyl phosphate), BHT.
- water-soluble polymers such as polyvinyl alcohol, and polyvinylpyrrolidone
- polysaccharides such as gum arabic, alginic acid and its salt, CMC (carboxymethylcellulose), and xanthan gum
- inorganic materials such as aluminum magnesium silicate, alumina sol
- preservatives coloring agents
- coloring agents coloring agents
- stabilizers such as PAP (acidic isopropyl phosphate), BHT.
- composition can be also prepared by formulating a “carboxamide compound” and “neonicotinoid compound(s)” according to the method as described in the above, and then making the formulations or their diluents.
- composition can be used for protecting plants from damage by pest (for example, insect pest and plant disease) which gives damage to the plant by feeding, sucking, or the like.
- pest for example, insect pest and plant disease
- insect pest which can be controlled by the “composition” include the followings.
- Hemiptera Planthoppers ( Delphacidae ) such as small brown planthopper ( Laodelphax striatellus ), brown rice planthopper ( Nilaparvata lugens ) and white-backed rice planthopper ( Sogatella furcifera ); leafhoppers ( Deltocephalidae ) such as green rice leafhopper ( Nephotettix cincticeps ), green rice leafhopper ( Nephotettix virescens ); aphids ( Aphididae ) such as cotton aphid ( Aphis gossypii ), green peach aphid ( Myzus persicae ), cabbage aphid ( Brevicoryne brassicae ), potato aphid ( Macrosiphum euphorbiae ), foxglove aphid ( Aulacorthum solani ), oat bird-cherry aphid ( Rhopalosiphum padi ), tropical citrus
- Lepidoptera Pyralid moths ( Pyralidae ) such as rice stem borer ( Chilo suppressalis ), yellow rice borer ( Tryporyza incertulas ), rice leafroller ( Cnaphalocrocis medinalis ), cotton leafroller ( Notarcha derogate ), Indian meal moth ( Plodia interpunctella ), oriental corn borer ( Ostrinia furnacalis ), cabbage webworm ( Hellula undalis ) and bluegrass webworm ( Pediasia teterrellus ); owlet moths ( Noctuidae ) such as common cutworm ( Spodoptera litura ), beet armyworm ( Spodoptera exigua ), armyworm ( Pseudaletia separate ), cabbage armyworm ( Mamestra brassicae ), black cutworm ( Agrotis ipsilon ), beet semi-looper ( Plusia nigrisigna ), Thoricoplusia ,
- yponomeutid moths such as diamondback moth ( Plutella xylostella ); gelechiid moths ( Gelechiidae ) such as pink bollworm ( Pectinophora gossypiella ) and potato tuberworm ( Phthorimaea operculella ); tiger moths and allies ( Arctiidae ) such as fall webworm ( Hyphantria cunea ); tineid moths ( Tineidae ) such as casemaking clothes moth ( Tinea translucens ) and webbing clothes moth ( Tineola bisselliella ); and the like,
- Thysanoptera Thrips ( Thripidae ) such as western flower thrips ( Frankliniella occidentalis ), melon thrips ( Thrips peri ), yellow tea thrips ( Scirtothrips dorsalis ), onion thrips ( Thrips tabaci ), flower thrips ( Frankliniella intonsa ), tobacco thrips( Frankliniella fusca );
- Diptera housefly ( Musca domestica ), common mosquito ( Culex pipiens pallens ), Tabanus ( Tabanus trigonus ), onion fly( Hylemya antiqua ), seed-corn fly( Hylemya platura ), Chinese anopheles ( Anopheles sinensis ), Japanese leaf miner ( Agromyza oryzae ), rice leafminer( Hydrellia griseola ), rice stem maggot ( Chlorops oryzae ), melon fly( Dacus cucurbitae ), mediterranean fruit fly( Ceratitis capitata ) and Liriomyza tritrifolii;
- Coleoptera 28-spotted ladybird( Epilachna vigintioctopunctata ), cucurbit leaf beetle( Aulacophora femoralis ), Phyllotreta striolata , rice leaf beetle( Oulema oryzae ), rice plant weevil( Echinocnemus squameus ), rice water weevil( Lissorhoptrus oryzophilus ), boll weevil( Anthonomus grandis ), adzuki bean weevil( Callosobruchus chinensis ), zoysia billbug( Sphenophorus venatus ), Japanese beetle ( Popillia japonica ), cupreous chafer(Anomala cuprea), corn rootworm families(Diabrotica spp.), Colorado potato beetle( Letinotarsa decemlineata ), beetle of family Elateridae ( Agriote
- Orthoptera grasshoppers ( Locusta migratoria ), mole cricket ( Gryllotalpa Africana ), Oxya yezoensis, Oxya japonica , and the like;
- Hymenoptera turnip sawfly ( Athalia rosae ), leafcutter ant( Acromyrmex spp.), fire ants( Solenopsis spp.), and the like;
- German cockroach Blattella germanica
- smokybrown cockroach Periplaneta fuliginosa
- American cockroach Periplaneta americana
- black Mississippi cockroach Periplaneta brunnea
- Oriental cockroach Blatta orientalis
- plant diseases which can be controlled by the “composition” include the followings.
- Wheat diseases Erysiphe graminis, Fusarium graminearum, F. avenaceum, F. culmorum, Microdochium nivale, Puccinia striiformis, P. graminis, P. recondita, Micronectriella nivale, Typhula sp., Ustilago tritici, Tilletia caries, Pseudocercosporella herpotrichoides, Mycosphaerella graminicola, Stagonospora nodorum, Pyrenophora tritici -repentis;
- Barley diseases Erysiphe graminis, Fusarium graminearum, F. avenaceum, F. culmorum, Microdochium nivale, Puccinia striiformis, P. graminis, P. hordei, Ustilago nuda, Rhynchosporium secalis, Pyrenophora teres, Cochliobolus sativus, Pyrenophora graminea, Rhizoctonia solani;
- Maize diseases Ustilago maydis, Cochliobolus heterostrophus, Gloeocercospora sorghi, Puccinia polysora, Cercospora zeae -maydis, Rhizoctonia solani;
- Citrus diseases Diaporthe citri, Elsinoe fawcetti, Penicillium digitatum, P. italicum, Phytophthora parasitica, Phytophthora citrophthora;
- Apple diseases Monilinia mali, Valsa ceratosperma, Podosphaera leucotricha, Alternaria alternata apple pathotype, Venturia inaequalis, Colletotrichum acutatum, Phytophtora cactorum;
- Pear diseases Venturia nashicola, V. pirina, Alternaria alternata Japanese pear pathotype, Gymnosporangium haraeanum, Phytophtora cactorum;
- Peach diseases Monilinia fructicola, Cladosporium carpophilum, Phomopsis sp.;
- Grape diseases Elsinoe ampelina, Glomerella cingulata, Uninula necator, Phakopsora ampelopsidis, Guignardia bidwellii, Plasmopara viticola; Persimmon diseases: Gloesporium kaki, Cercospora kaki, Mycosphaerela nawae; Gourd diseases: Colletotrichum lagenarium, Sphaerotheca fuliginea, Mycosphaerella melonis, Fusarium oxysporum, Pseudoperonospora cubensis, Phytophthora sp., Pythium sp.;
- Tomato diseases Alternaria solani, Cladosporium fulvum, Phytophthora infestans;
- Brassicaceous vegetable diseases Alternaria japonica, Cercosporella brassicae, Plasmodiophora brassicae, Peronospora parasitica;
- Soybean diseases Cercospora kikuchii, Elsinoe glycines, Diaporthe phaseolorum var. sojae, Septoria glycines, Cercospora sojina, Phakopsora pachyrhizi, Phytophthora sojae, Rhizoctonia solani, Corynespora casiicola, Sclerotinia sclerotiorum;
- Kidney bean diseases Colletrichum lindemthianum
- Peanut diseases Cercospora personata, Cercospora arachidicola, Sclerotium rolfsii;
- Potato diseases Alternaria solani, Phytophthora infestans, Phytophthora erythroseptica, Spongospora subterranean , f. sp. Subterranean;
- Tea diseases Exobasidium reticulatum, Elsinoe leucospila, Pestalotiopsis sp., Colletotrichum theae - sinensis;
- Tobacco diseases Alternaria longipes, Erysiphe cichoracearum, Colletotrichum tabacum, Peronospora tabacina, Phytophthora nicotianae;
- Rapeseed diseases Sclerotinia sclerotiorum, Rhizoctonia solani;
- Zoysia diseases Sclerotinia homeocarpa, Rhizoctonia solani;
- Banana diseases Mycosphaerella fijiensis, Mycosphaerella musicola;
- Agricultural crops maize, rice, wheat, barley, rye, oat, sorghum, cotton, soybean, peanut, buckwheat, sugar beet, rapeseed, sunflower, sugar cane, tobacco, and the like;
- Vegetables Solanaceous vegetables (eggplant, tomato, green pepper, hot pepper, potato, etc.), Cucurbitaceous vegetables (cucumber, pumpkin, zucchini, watermelon, melon, squash, etc.); Cruciferous vegetables (radish, turnip, horseradish, kohlrabi, Chinese cabbage, cabbage, brown mustard, broccoli, cauliflower, etc.), Asteraceous vegetables (burdock, garland chrysanthemum, artichoke, lettuce, etc.), Liliaceous vegetables (Welsh onion, onion, garlic, asparagus, etc.), Umbelliferous vegetables (carrot, parsley, celery, parsnip, etc.), Chenopodiaceous vegetables (spinach, chard, etc.), Lamiaceous vegetables (Japanese basil, mint, basil, etc.), strawberry, sweet potato, yam, aroid, and the like;
- Fruit trees pome fruits (apple, common pear, Japanese pear, Chinese quince, quince, etc.), stone fruits (peach, plum, nectarine, Japanese plum, cherry, apricot, prune, etc.), citrus (mandarin, orange, lemon, lime, grapefruit, etc.), nuts (chestnut, walnut, hazel nut, almond, pistachio, cashew nut, macadamia nut, etc.), berry fruits (blueberry, cranberry, blackberry, raspberry, etc.), grape, persimmon, olive, loquat, banana, coffee, date, coconut palm, and the like;
- Trees other than fruit trees tea, mulberry, flowering trees, street trees (ash tree, birch, dogwood, eucalyptus, ginkgo, lilac, maple tree, oak, poplar, cercis, Chinese sweet gum, plane tree, zelkova, Japanese arborvitae, fir tree, Japanese hemlock, needle juniper, pine, spruce, yew), and the like.
- the above-described plants may be those having resistance imparted by genetic engineering technique.
- the “composition” is expected to have excellent controlling effect particularly to plant disease caused in soybean.
- soybean diseases to which especially excellent effect of the “composition” can be expected are Rhizoctonia solani, Cercospora kikuchii, Septoria glycines, Corynespora casiicola, Phakopsora pachyrizi, Sclerotinia sclerotiorum, Cercospora sojina , and the like.
- compositions exemplify an embodiment of the “composition”:
- composition comprising “carboxamide compound (1)” and clothianidin;
- composition comprising “carboxamide compound (1)” and imidacloprid;
- composition comprising “carboxamide compound (1)” and thiamethoxam;
- composition comprising “carboxamide compound (2)” and clothianidin;
- composition comprising “carboxamide compound (2)” and imidacloprid;
- composition comprising “carboxamide compound (2)” and thiamethoxam;
- composition comprising “carboxamide compound (3)” and clothianidin;
- composition comprising “carboxamide compound (3)” and imidacloprid;
- composition comprising “carboxamide compound (3)” and thiamethoxam;
- composition comprising “carboxamide compound (4)” and clothianidin;
- composition comprising “carboxamide compound (4)” and imidacloprid;
- composition comprising “carboxamide compound (4)” and thiamethoxam;
- composition comprising “carboxamide compound (5)” and clothianidin;
- composition comprising “carboxamide compound (5)” and imidacloprid;
- composition comprising “carboxamide compound (5)” and thiamethoxam;
- composition comprising “carboxamide compound (1)” and clothianidin in which the weight ratio of “carboxamide compound (1)” to clothianidin is 0.01/1 to 4/1;
- composition comprising “carboxamide compound (1)” and imidacloprid;
- composition comprising “carboxamide compound (1)” and thiamethoxam in which the weight ratio of “carboxamide compound (1)” to thiamethoxam is 0.01/1 to 4/1;
- composition comprising “carboxamide compound (2)” and clothianidin in which the weight ratio of “carboxamide compound (2)” to clothianidin is 0.01/1 to 4/1;
- composition comprising “carboxamide compound (2)” and imidacloprid;
- composition comprising “carboxamide compound (2)” and thiamethoxam in which the weight ratio of “carboxamide compound (2)” to thiamethoxam is 0.01/1 to 4/1;
- composition comprising “carboxamide compound (3)” and clothianidin in which the weight ratio of “carboxamide compound (3)” to clothianidin is 0.01/1 to 4/1;
- composition comprising “carboxamide compound (3)” and imidacloprid;
- composition comprising “carboxamide compound (3)” and thiamethoxam in which the weight ratio of “carboxamide compound (3)” to thiamethoxam is 0.01/1 to 4/1;
- composition comprising “carboxamide compound (4)” and clothianidin in which the weight ratio of “carboxamide compound (4)” to clothianidin is 0.01/1 to 4/1;
- composition comprising “carboxamide compound (4)” and imidacloprid
- composition comprising “carboxamide compound (4)” and thiamethoxam in which
- the weight ratio of “carboxamide compound (4)” to thiamethoxam is 0.01/1 to 4/1;
- composition comprising “carboxamide compound (5)” and clothianidin in which the weight ratio of “carboxamide compound (5)” to clothianidin is 0.01/1 to 4/1;
- composition comprising “carboxamide compound (5)” and imidacloprid;
- composition comprising “carboxamide compound (5)” and thiamethoxam in which the weight ratio of “carboxamide compound (5)” to thiamethoxam is 0.01/1 to 4/1.
- controlling method can be carried out by treating a plant or the soil where a plant grows with an effective amount of a “carboxamide compound” and “neonicotinoid compound(s)”.
- the part of plant to be treated is stem and leaf of a plant, seed or bulb of a plant, and the bulb means bulb, corm, rootstock, tuber, tuberous root and rhizophore.
- the treatment of a plant or the soil where a plant grows with a “carboxamide compound” and “neonicotinoid compound(s)” can be carried out separately at the same timing, but the treatment is usually carried out by using a “composition” in light of convenience.
- the treatment with a carboxamide compound” and “neonicotinoid compound(s)” is, for example, stems and leaves application, soil application, roots application or seeds application.
- Examples of the stems and leaves application include a treatment for surface of cultivated plant by a stem and leave spray or a stem and tree spray.
- Examples of the root application include a method of dipping a whole plant or the root of a plant into a liquid containing a “carboxamide compound” and “neonicotinoid compound(s)” and a method of sticking a solid preparation comprising a “carboxamide compound”, “neonicotinoid compound(s)” and a solid carrier onto the root of a plant.
- Examples of the soil application include a method of spraying a “composition” onto a soil, a method of mixing a “composition” with a soil and a method of irrigating a “composition” into the soil.
- the seed application examples include a method of treating seeds or bulbs of a plant to be protected from a plant disease with a “composition”
- the application can be carried out by spraying a suspension of a “composition” to the surface of seeds or bulbs, or by spreading wettable powder, emulsifiable concentrate or flowable formulation itself or a mixture thereof with a small amount of water on the seeds or the bulbs, or by dipping the seeds into a solution of a “composition” for a prescribed time, by film coating application or pellet coating application.
- the amount of a “carboxamide compound” and “neonicotinoid compound(s)” used in the “controlling method” is different depending on the kind of a plant to be treated, the kind of a plant disease to be controlled and its frequency, the kind of a formulation, timing of treatment, method of treatment, place of treatment, weather condition, and the like.
- the total amount of a “carboxamide compound” and “neonicotinoid compound(s)” is usually from 1 g to 500 g/1000 m 2 , preferably from 2 g to 200 g/1000 m 2 and more preferably from 10 g to 100 g/1000 m 2 .
- the total amount of a “carboxamide compound” and “neonicotinoid compound(s)” is usually from 0.001 g to 10 g/1 kg of the seeds, and preferably from 0.01 g to 1 g/1 kg of the seeds.
- An emulsifiable concentrate, wettable powder or flowable formulation is usually by diluting the formulation with a small amount of water and spraying the diluted formulation.
- concentration of a “carboxamide compound” and “neonicotinoid compound(s)” in total of the diluted formulation is usually from 0.0005 to 2% by weight and preferably from 0.005 to 1% by weight.
- a powder formulation or granule formulation and the like is usually used without dilution.
- part means “part by weight” unless otherwise provided.
- One of the “carboxamide compound” (1) to (5) (5 parts), clothianidin (10 parts), sorbitan trioleate (1.5 parts), and an aqueous solution (28.5 parts) containing polyvinyl alcohol (2 parts) are mixed and the mixture is milled by wet-milling method.
- propylene glycol (10 parts) is added to the mixture by stirring to give each of flowable formulations, respectively.
- One of the “carboxamide compound” (1) to (5) (2 parts), thiamethoxam (8 parts), a mixture of white carbon and polyoxyethylene alkyl ether sulfate ammonium salt (weight ratio 1:1)(35 parts) and water (55 parts) are mixed and the mixture is milled by wet-milling method to give each of flowable formulations, respectively.
- One of the “carboxamide compound” (1) to (5) (2 parts), imidacloprid (8 parts), a mixture of white carbon and polyoxyethylene alkyl ether sulfate ammonium salt (weight ratio 1:1)(35 parts) and water (55 parts) are mixed and the mixture is milled by wet-milling method to give each of flowable formulations, respectively.
- One of the “carboxamide compound” (1) to (5) (5 parts), imidacloprid (10 parts), sorbitan trioleate (1.5 parts), water (28.5 parts) containing polyvinyl alcohol (2 parts) are mixed and the mixture is milled by wet-milling method. An aqueous solution (45 parts) containing xanthan gum (0.05 part) and aluminum magnesium silicate (0.1 part) is added to the milled mixture. To the mixture is added propylene glycol (10 parts) and the resultant mixture is mixed by stirring to give each of flowable formulations, respectively.
- a cyclohexanone solution (100microL) containing prescribed amount (weight) of a test compound was applied on seeds of soybean (variety : Natto shoryu) (10 g) by using a rotary apparatus for seed treatment (Seed dresser, manufactured by Hans-Ulrich Hege GmbH).
- treated plot One day after the application, plastic pot was filled with soil contaminated by Rhizoctonia solani , and the seeds treated with the test compounds were seeded in the soil and cultivated in a glass-greenhouse for 20 days (hereinafter referred to as “treated plot”).
- non-treated plot seeds of soybean which were not treated as above were cultivated in the same way as above (hereinafter referred to as “non-treated plot”) and the disease severity in “non-treated plot” was calculated in the same way as the above “treated plot”.
- efficacy in the “treated plot” was evaluated according to the following calculation formula (2).
- a pesticidal composition comprising a carboxamide compound represented by formula (I) and one or more neonicotinoid compounds selected from group (A) is useful for controlling pests.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2010-101851 | 2010-04-27 | ||
JP2010101851A JP5782678B2 (ja) | 2010-04-27 | 2010-04-27 | 有害生物防除組成物およびその用途 |
PCT/JP2011/002413 WO2011135830A1 (en) | 2010-04-27 | 2011-04-25 | Pesticidal composition and its use |
Publications (2)
Publication Number | Publication Date |
---|---|
US20130045970A1 US20130045970A1 (en) | 2013-02-21 |
US8691812B2 true US8691812B2 (en) | 2014-04-08 |
Family
ID=44861152
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US13/643,576 Active US8691812B2 (en) | 2010-04-27 | 2011-04-25 | Pesticidal composition and its use |
Country Status (18)
Country | Link |
---|---|
US (1) | US8691812B2 (zh) |
EP (1) | EP2563132B1 (zh) |
JP (1) | JP5782678B2 (zh) |
KR (1) | KR101811898B1 (zh) |
CN (1) | CN102858166B (zh) |
AR (1) | AR083145A1 (zh) |
AU (1) | AU2011246795B2 (zh) |
BR (1) | BR112012027384B1 (zh) |
CA (1) | CA2797218C (zh) |
CL (1) | CL2012002972A1 (zh) |
CO (1) | CO6571877A2 (zh) |
MX (1) | MX2012012305A (zh) |
MY (1) | MY156565A (zh) |
NZ (1) | NZ603840A (zh) |
RU (1) | RU2556402C2 (zh) |
TW (1) | TWI486125B (zh) |
UA (1) | UA107830C2 (zh) |
WO (1) | WO2011135830A1 (zh) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ITMI20121045A1 (it) | 2012-06-15 | 2013-12-16 | Isagro Ricerca Srl | Composizioni sinergiche per la protezione di colture agrarie e relativo uso |
CA2892699C (en) | 2012-11-30 | 2023-01-24 | Bayer Cropscience Ag | Ternary fungicidal combinations comprising pyrazole carboxamides |
EA201500580A1 (ru) * | 2012-11-30 | 2016-01-29 | Байер Кропсайенс Акциенгезельшафт | Двойные фунгицидные смеси |
CN104837351A (zh) | 2012-11-30 | 2015-08-12 | 拜耳作物科学股份公司 | 二元杀真菌或杀虫混合物 |
EA030020B1 (ru) | 2012-11-30 | 2018-06-29 | Байер Кропсайенс Акциенгезельшафт | Двойные фунгицидные смеси |
EA030236B1 (ru) * | 2012-11-30 | 2018-07-31 | Байер Кропсайенс Акциенгезельшафт | Тройные фунгицидные и пестицидные смеси |
TWI607005B (zh) * | 2013-01-31 | 2017-12-01 | 住友化學股份有限公司 | 有害生物防治組成物及有害生物之防治方法 |
CN106417319A (zh) * | 2016-06-30 | 2017-02-22 | 京博农化科技股份有限公司 | 一种含吡蚜酮的杀虫组合物 |
AR114466A1 (es) | 2018-04-04 | 2020-09-09 | Fmc Corp | Formulaciones de concentrados emulsionables de fungicidas de sdhi |
Citations (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4536506A (en) | 1981-12-01 | 1985-08-20 | Rhone-Poulenc Agrochimie | Insecticidal and acaricidal combination containing a pyrethroid |
WO1986002641A1 (en) | 1984-10-29 | 1986-05-09 | Sumitomo Chemical Company, Limited | Pyrazolecarboxamide derivatives, process for their preparation, and bactericides containing them as effective ingredients |
JPS6296472A (ja) | 1985-10-22 | 1987-05-02 | Sumitomo Chem Co Ltd | ピラゾ−ルカルボキサミド誘導体およびそれを有効成分とする殺菌剤 |
US5093347A (en) | 1991-01-28 | 1992-03-03 | Monsanto Company | 3-difluoromethylpyrazolecarboxamide fungicides, compositions and use |
WO1995027693A1 (fr) | 1994-04-06 | 1995-10-19 | Shionogi & Co., Ltd. | DERIVE D'ACIDE PHENYLACETIQUE A SUBSTITUTION α, SON PROCEDE D'OBTENTION ET BACTERICIDE AGRICOLE LE CONTENANT |
WO2004067528A1 (en) | 2003-01-28 | 2004-08-12 | E.I. Du Pont De Nemours And Company | Cyano anthranilamide insecticides |
WO2005077934A1 (ja) | 2004-02-18 | 2005-08-25 | Ishihara Sangyo Kaisha, Ltd. | アントラニルアミド系化合物、それらの製造方法及びそれらを含有する有害生物防除剤 |
JP3729825B2 (ja) | 2001-08-13 | 2005-12-21 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 殺節足動物性アントラニルアミド |
JP2007182422A (ja) | 2005-10-14 | 2007-07-19 | Sumitomo Chemical Co Ltd | ヒドラジド化合物およびその有害生物防除用途 |
WO2007095229A2 (en) | 2006-02-10 | 2007-08-23 | Dow Agrosciences Llc | Insecticidal n-substituted (6-haloalkylpyridin-3-yl)alkyl sulfoximines |
WO2007108483A1 (ja) | 2006-03-20 | 2007-09-27 | Nihon Nohyaku Co., Ltd. | N-2-(ヘテロ)アリールエチルカルボキサミド誘導体及びこれを含有する有害生物防除剤 |
WO2008046533A2 (en) | 2006-10-19 | 2008-04-24 | Bayer Cropscience Ag | Fungicidal and insecticidal composition |
WO2008069990A1 (en) | 2006-12-01 | 2008-06-12 | E. I. Du Pont De Nemours And Company | Liquid formulations of carboxamide arthropodicides |
JP4150379B2 (ja) | 2004-02-18 | 2008-09-17 | 石原産業株式会社 | アントラニルアミド系化合物、それらの製造方法及びそれらを含有する有害生物防除剤 |
WO2008126933A2 (en) | 2007-04-11 | 2008-10-23 | Sumitomo Chemical Company, Limited | Process for producing pesticidal benzamide compounds |
JP2009502747A (ja) | 2005-07-14 | 2009-01-29 | ビーエーエスエフ ソシエタス・ヨーロピア | 1−メチル−ピラゾール−4−イルカルボキシアニリド類に基づく殺菌性混合物 |
US20090181956A1 (en) | 2005-10-14 | 2009-07-16 | Hiroshi Ikegami | Hydrazide Compound and Pesticidal Use of the Same |
EP2100505A1 (en) | 2006-11-21 | 2009-09-16 | Mitsui Chemicals Agro, Inc. | Composition for controlling plant disease and insect damage and method for preventing plant disease and insect damage |
WO2009119872A2 (en) | 2008-03-28 | 2009-10-01 | Sumitomo Chemical Company, Limited | Plant disease controlling composition and method for controlling plant disease |
JP2010013389A (ja) | 2008-07-03 | 2010-01-21 | Nissan Chem Ind Ltd | 水中溶出性が促進される農薬組成物 |
WO2010021404A2 (en) | 2008-08-19 | 2010-02-25 | Ishihara Sangyo Kaisha, Ltd. | Method for controlling degradation of agricultural chemical active ingredient |
WO2010024365A1 (en) | 2008-08-26 | 2010-03-04 | Sumitomo Chemical Company, Limited | Amide compounds and use thereof |
WO2010024422A1 (en) | 2008-08-26 | 2010-03-04 | Sumitomo Chemical Company, Limited | Amide compounds and use thereof |
JP2010083869A (ja) | 2008-09-08 | 2010-04-15 | Nissan Chem Ind Ltd | 水田水口施用農薬包装袋 |
JP2010083883A (ja) | 2008-09-08 | 2010-04-15 | Nissan Chem Ind Ltd | イソキサゾリン置換ベンズアミド化合物及び有害生物防除剤 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102005045174A1 (de) * | 2005-09-21 | 2007-03-22 | Bayer Cropscience Ag | Steigerung der Pathogenabwehr in Pflanzen |
CA2728887A1 (en) | 2008-07-04 | 2010-01-07 | Basf Se | Fungicidal mixtures comprising substituted 1-methylpyrazol-4-ylcarboxanilides |
-
2010
- 2010-04-27 JP JP2010101851A patent/JP5782678B2/ja active Active
-
2011
- 2011-04-25 UA UAA201213553A patent/UA107830C2/ru unknown
- 2011-04-25 RU RU2012150500/13A patent/RU2556402C2/ru active
- 2011-04-25 NZ NZ603840A patent/NZ603840A/en unknown
- 2011-04-25 BR BR112012027384-1A patent/BR112012027384B1/pt active IP Right Grant
- 2011-04-25 EP EP11774616.4A patent/EP2563132B1/en not_active Not-in-force
- 2011-04-25 CN CN201180020841.3A patent/CN102858166B/zh active Active
- 2011-04-25 MY MYPI2012004303A patent/MY156565A/en unknown
- 2011-04-25 TW TW100114310A patent/TWI486125B/zh active
- 2011-04-25 US US13/643,576 patent/US8691812B2/en active Active
- 2011-04-25 MX MX2012012305A patent/MX2012012305A/es active IP Right Grant
- 2011-04-25 AU AU2011246795A patent/AU2011246795B2/en active Active
- 2011-04-25 CA CA2797218A patent/CA2797218C/en active Active
- 2011-04-25 KR KR1020127028132A patent/KR101811898B1/ko active IP Right Grant
- 2011-04-25 WO PCT/JP2011/002413 patent/WO2011135830A1/en active Application Filing
- 2011-04-27 AR ARP110101446A patent/AR083145A1/es active IP Right Grant
-
2012
- 2012-10-24 CL CL2012002972A patent/CL2012002972A1/es unknown
- 2012-10-30 CO CO12195295A patent/CO6571877A2/es active IP Right Grant
Patent Citations (41)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4536506A (en) | 1981-12-01 | 1985-08-20 | Rhone-Poulenc Agrochimie | Insecticidal and acaricidal combination containing a pyrethroid |
WO1986002641A1 (en) | 1984-10-29 | 1986-05-09 | Sumitomo Chemical Company, Limited | Pyrazolecarboxamide derivatives, process for their preparation, and bactericides containing them as effective ingredients |
US4742074A (en) | 1984-10-29 | 1988-05-03 | Sumitomo Chemical Company, Limited | Pyrazolecarboxamide derivative and fungicide containing it as active ingredient |
JPS6296472A (ja) | 1985-10-22 | 1987-05-02 | Sumitomo Chem Co Ltd | ピラゾ−ルカルボキサミド誘導体およびそれを有効成分とする殺菌剤 |
US5093347A (en) | 1991-01-28 | 1992-03-03 | Monsanto Company | 3-difluoromethylpyrazolecarboxamide fungicides, compositions and use |
WO1992012970A1 (en) | 1991-01-28 | 1992-08-06 | Monsanto Company | 3-difluoromethylpyrazolecarboxamide fungicides |
WO1995027693A1 (fr) | 1994-04-06 | 1995-10-19 | Shionogi & Co., Ltd. | DERIVE D'ACIDE PHENYLACETIQUE A SUBSTITUTION α, SON PROCEDE D'OBTENTION ET BACTERICIDE AGRICOLE LE CONTENANT |
US5948819A (en) | 1994-04-06 | 1999-09-07 | Shionogi & Co., Ltd | α-substituted phenylacetic acid derivative, its production and agricultural fungicide containing it |
JP3729825B2 (ja) | 2001-08-13 | 2005-12-21 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 殺節足動物性アントラニルアミド |
US7232836B2 (en) | 2001-08-13 | 2007-06-19 | E. I. Du Pont De Nemours And Company | Arthropodicidal anthranilamides |
US20120171183A1 (en) | 2001-08-13 | 2012-07-05 | E.I. Du Pont De Nemours And Company | Arthropodicidal anthranilamides |
US8158802B2 (en) | 2001-08-13 | 2012-04-17 | E.I. Du Pont De Nemours And Company | Arthropodicidal anthranilamides |
US8148521B2 (en) | 2001-08-13 | 2012-04-03 | E.I. Du Pont De Nemours And Company | Arthropodicidal anthranilamides |
US7902231B2 (en) | 2001-08-13 | 2011-03-08 | E.I. Du Pont De Nemours And Company | Anthropodicidal anthranilamides |
WO2004067528A1 (en) | 2003-01-28 | 2004-08-12 | E.I. Du Pont De Nemours And Company | Cyano anthranilamide insecticides |
WO2005077934A1 (ja) | 2004-02-18 | 2005-08-25 | Ishihara Sangyo Kaisha, Ltd. | アントラニルアミド系化合物、それらの製造方法及びそれらを含有する有害生物防除剤 |
US20110257231A1 (en) | 2004-02-18 | 2011-10-20 | Ishihara Sangyo Kaisha Ltd. | Anthranilamide compounds, process for their production and pesticides containing them |
US7994201B2 (en) | 2004-02-18 | 2011-08-09 | Ishihara Sangyo Kaisha, Ltd. | Anthranilamide compounds, process for their production and pesticides containing them |
JP4150379B2 (ja) | 2004-02-18 | 2008-09-17 | 石原産業株式会社 | アントラニルアミド系化合物、それらの製造方法及びそれらを含有する有害生物防除剤 |
US7612100B2 (en) | 2004-02-18 | 2009-11-03 | Ishihara Sangyo Kaisha, Ltd. | Anthranilamides, process for the production thereof, and pest controllers containing the same |
JP2009502747A (ja) | 2005-07-14 | 2009-01-29 | ビーエーエスエフ ソシエタス・ヨーロピア | 1−メチル−ピラゾール−4−イルカルボキシアニリド類に基づく殺菌性混合物 |
US20090123561A1 (en) | 2005-07-14 | 2009-05-14 | Basf Aktiengeselllschaft | Fungicide mixtures based on 1-methyl-pyrazol-4-ylcarboxanilides |
US20090181956A1 (en) | 2005-10-14 | 2009-07-16 | Hiroshi Ikegami | Hydrazide Compound and Pesticidal Use of the Same |
JP2007182422A (ja) | 2005-10-14 | 2007-07-19 | Sumitomo Chemical Co Ltd | ヒドラジド化合物およびその有害生物防除用途 |
WO2007095229A2 (en) | 2006-02-10 | 2007-08-23 | Dow Agrosciences Llc | Insecticidal n-substituted (6-haloalkylpyridin-3-yl)alkyl sulfoximines |
WO2007108483A1 (ja) | 2006-03-20 | 2007-09-27 | Nihon Nohyaku Co., Ltd. | N-2-(ヘテロ)アリールエチルカルボキサミド誘導体及びこれを含有する有害生物防除剤 |
WO2008046533A2 (en) | 2006-10-19 | 2008-04-24 | Bayer Cropscience Ag | Fungicidal and insecticidal composition |
US20100056594A1 (en) | 2006-11-21 | 2010-03-04 | Mitsui Chemicals, Inc. | Plant disease and insect damage control composition, and plant disease and insect damage prevention method |
EP2100505A1 (en) | 2006-11-21 | 2009-09-16 | Mitsui Chemicals Agro, Inc. | Composition for controlling plant disease and insect damage and method for preventing plant disease and insect damage |
WO2008069990A1 (en) | 2006-12-01 | 2008-06-12 | E. I. Du Pont De Nemours And Company | Liquid formulations of carboxamide arthropodicides |
US20100055084A1 (en) | 2006-12-01 | 2010-03-04 | E.I. Du Pont De Nemours And Company | Liquid formulations of carboxamide arthropodicides |
US20100120866A1 (en) | 2007-04-11 | 2010-05-13 | Sumitomo Chemical Company, Limited | Process for producing amide compound |
WO2008126933A2 (en) | 2007-04-11 | 2008-10-23 | Sumitomo Chemical Company, Limited | Process for producing pesticidal benzamide compounds |
JP2008280335A (ja) | 2007-04-11 | 2008-11-20 | Sumitomo Chemical Co Ltd | アミド化合物の製造方法 |
WO2009119872A2 (en) | 2008-03-28 | 2009-10-01 | Sumitomo Chemical Company, Limited | Plant disease controlling composition and method for controlling plant disease |
JP2010013389A (ja) | 2008-07-03 | 2010-01-21 | Nissan Chem Ind Ltd | 水中溶出性が促進される農薬組成物 |
WO2010021404A2 (en) | 2008-08-19 | 2010-02-25 | Ishihara Sangyo Kaisha, Ltd. | Method for controlling degradation of agricultural chemical active ingredient |
WO2010024422A1 (en) | 2008-08-26 | 2010-03-04 | Sumitomo Chemical Company, Limited | Amide compounds and use thereof |
WO2010024365A1 (en) | 2008-08-26 | 2010-03-04 | Sumitomo Chemical Company, Limited | Amide compounds and use thereof |
JP2010083869A (ja) | 2008-09-08 | 2010-04-15 | Nissan Chem Ind Ltd | 水田水口施用農薬包装袋 |
JP2010083883A (ja) | 2008-09-08 | 2010-04-15 | Nissan Chem Ind Ltd | イソキサゾリン置換ベンズアミド化合物及び有害生物防除剤 |
Non-Patent Citations (21)
Title |
---|
Colombian Office Action dated Jul. 16, 2013 for Colombian Application No. 12-195295-4. |
Delp, "Coping with Resistance to Plant Disease," Plant Disease, vol. 64, No. 7, Jul. 1980, pp. 652-657. |
International Search Report for International Patent Application No. PCT/JP2011/002410, dated Jun. 28, 2011. |
International Search Report for International Patent Application No. PCT/JP2011/002411, dated Jul. 5, 2011. |
International Search Report for International Patent Application No. PCT/JP2011/002413, dated Jul. 19, 2011. |
International Search Report for International Patent Application No. PCT/JP2011/002414, dated Jul. 12, 2011. |
International Search Report for International Patent Application No. PCT/JP2011/002415, dated Jul. 19, 2011. |
International Search Report for International Patent Application No. PCT/JP2011/002416, dated May 31, 2011. |
International Search Report for International Patent Application No. PCT/JP2011/002417, dated Jul. 26, 2011. |
International Search Report for International Patent Application No. PCT/JP2011/002418, dated May 31, 2011. |
International Search Report for International Patent Application No. PCT/JP2011/002419, dated May 31, 2011. |
International Search Report for International Patent Application No. PCT/JP2011/002420, dated May 31, 2011. |
International Search Report for International Patent Application No. PCT/JP2011/002421, dated May 31, 2011. |
International Search Report for International Patent Application No. PCT/JP2011/002422, dated May 31, 2011. |
International Search Report for International Patent Application No. PCT/JP2011/002423, dated Jul. 19, 2011. |
Office Action for U.S. Appl. No. 13/643,577, dated Jun. 11, 2013. |
Office Action for U.S. Appl. No. 13/643,818, dated Aug. 20, 2013. |
Office Action for U.S. Appl. No. 13/643,846, dated Aug. 7, 2013. |
Office Action for U.S. Appl. No. 13/643,913, dated Apr. 26, 2013. |
Office Action for U.S. Appl. No. 13/643,960, dated Aug. 1, 2013. |
The Supplementary Search Report, dated Aug. 27, 2013, issued in corresponding European Patent Application No. 11774616.4. |
Also Published As
Publication number | Publication date |
---|---|
CA2797218A1 (en) | 2011-11-03 |
US20130045970A1 (en) | 2013-02-21 |
CO6571877A2 (es) | 2012-11-30 |
BR112012027384A2 (pt) | 2015-09-15 |
JP5782678B2 (ja) | 2015-09-24 |
RU2012150500A (ru) | 2014-06-10 |
CA2797218C (en) | 2018-08-07 |
KR20130064062A (ko) | 2013-06-17 |
JP2011231041A (ja) | 2011-11-17 |
EP2563132B1 (en) | 2016-08-10 |
BR112012027384B1 (pt) | 2019-02-05 |
CN102858166A (zh) | 2013-01-02 |
TWI486125B (zh) | 2015-06-01 |
RU2556402C2 (ru) | 2015-07-10 |
MY156565A (en) | 2016-03-15 |
MX2012012305A (es) | 2012-11-23 |
EP2563132A1 (en) | 2013-03-06 |
KR101811898B1 (ko) | 2017-12-22 |
UA107830C2 (en) | 2015-02-25 |
AR083145A1 (es) | 2013-02-06 |
AU2011246795B2 (en) | 2015-07-09 |
TW201206348A (en) | 2012-02-16 |
CN102858166B (zh) | 2014-05-28 |
NZ603840A (en) | 2014-09-26 |
EP2563132A4 (en) | 2013-09-25 |
CL2012002972A1 (es) | 2013-03-22 |
WO2011135830A1 (en) | 2011-11-03 |
AU2011246795A1 (en) | 2012-10-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2563130B1 (en) | Pesticidal composition and its use | |
EP2563131B1 (en) | Pesticidal composition and its use | |
US9363998B2 (en) | Pesticidal composition and its use | |
EP2563133B1 (en) | Pesticidal composition and its use | |
US8691812B2 (en) | Pesticidal composition and its use | |
EP2563134B1 (en) | Pesticidal composition and its use | |
US9232798B2 (en) | Pesticidal composition and its use |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: SUMITOMO CHEMICAL COMPANY, LIMITED, JAPAN Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:MATSUZAKI, YUICHI;REEL/FRAME:029251/0269 Effective date: 20121024 |
|
FEPP | Fee payment procedure |
Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY |
|
STCF | Information on status: patent grant |
Free format text: PATENTED CASE |
|
MAFP | Maintenance fee payment |
Free format text: PAYMENT OF MAINTENANCE FEE, 4TH YEAR, LARGE ENTITY (ORIGINAL EVENT CODE: M1551) Year of fee payment: 4 |
|
MAFP | Maintenance fee payment |
Free format text: PAYMENT OF MAINTENANCE FEE, 8TH YEAR, LARGE ENTITY (ORIGINAL EVENT CODE: M1552); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY Year of fee payment: 8 |